Canonical Allele Identifier: CA913191166

Gene: GRN

Linked Data

• ClinVar Variation Id: 631772
• ClinVar RCV Id: RCV000778498
• dbSNP Id: rs1567887576
• gnomAD v4: 17-44351697-AAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351703_44351704del , CM000679.2:g.44351703_44351704del	GRCh38
NC_000017.10:g.42429071_42429072del , CM000679.1:g.42429071_42429072del	GRCh37
NC_000017.9:g.39784597_39784598del	NCBI36
NG_007886.1:g.11581_11582del , LRG_661:g.11581_11582del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1087_1088del MANE Select	ENSP00000053867.2:p.Asp363CysfsTer4
ENST00000639447.1:c.1087_1088del	ENSP00000492014.1:p.Asp363CysfsTer4
ENST00000053867.7:c.1087_1088del	ENSP00000053867.2:p.Asp363CysfsTer4
ENST00000586443.1:c.528_529del
ENST00000589265.5:c.616_617del	ENSP00000467616.1:p.Asp206CysfsTer4
ENST00000589923.1:n.345_346del
NM_002087.3:c.1087_1088del	NP_002078.1:p.Asp363CysfsTer4
XM_005257253.1:c.1087_1088del	XP_005257310.1:p.Asp363CysfsTer4
XM_024450730.1:c.1087_1088del	XP_024306498.1:p.Asp363CysfsTer4
NM_002087.4:c.1087_1088del MANE Select	NP_002078.1:p.Asp363CysfsTer4